Clinical outcomes of medical treatments for progressive desmoid tumors following active surveillance: a systematic review-Reference-Cited by-同舟云学术

Clinical outcomes of medical treatments for progressive desmoid tumors following active surveillance: a systematic review

Published:2022-02-12 Issue:1 Volume:107 Page:7-18
ISSN:2035-5106
Container-title:MUSCULOSKELETAL SURGERY
language:en
Short-container-title:Musculoskelet Surg

Author:

Tsukamoto S.^ORCID,Takahama T.,Mavrogenis A. F.,Tanaka Y.,Tanaka Y.,Errani C.

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine,Surgery

Link

https://link.springer.com/content/pdf/10.1007/s12306-022-00738-x.pdf

Reference55 articles.

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2. Kasper B, Baumgarten C, Bonvalot S et al (2015) Management of sporadic desmoid-type fibromatosis: a European consensus approach based on patients’ and professionals’ expertise - a sarcoma patients EuroNet and European organisation for research and treatment of cancer/soft tissue and bone sarcoma group initiative. Eur J Cancer 51:127–136. https://doi.org/10.1016/j.ejca.2014.11.005

3. Fiore M, Rimareix F, Mariani L et al (2009) Desmoid-type fibromatosis: a front-line conservative approach to select patients for surgical treatment. Ann Surg Oncol 16:2587–2593. https://doi.org/10.1245/s10434-009-0586-2

4. Penel N, Le Cesne A, Bonvalot S et al (2017) Surgical versus non-surgical approach in primary desmoid-type fibromatosis patients: a nationwide prospective cohort from the French Sarcoma Group. Eur J Cancer 83:125–131. https://doi.org/10.1016/j.ejca.2017.06.017

5. Orbach D, Brennan B, Bisogno G et al (2017) The EpSSG NRSTS 2005 treatment protocol for desmoid-type fibromatosis in children: an international prospective case series. Lancet Child Adolesc Health 1:284–292. https://doi.org/10.1016/S2352-4642(17)30045-7

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